Authors: Lossi, AM Colleaux, L Chiaroni, P Fontes, M Villard, L Abidi, F Schwartz, C Briault, S Moraine, C

Citation: Am. Lossi et al., Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three families, AM J MED G, 94(5), 2000, pp. 386-388

Authors: Villard, L Belougne, J Lossi, AM Fontes, M Colleaux, L

Citation: L. Villard et al., Transcript map of the human chromosome Xq11-Xq21 region: localization of 33 novel genes and one pseudogene, GENE, 235(1-2), 1999, pp. 43-50

Authors: Villard, L Bonino, MC Abidi, F Ragusa, A Belougne, J Lossi, AM Seaver, L Bonnefont, JP Romano, C Fichera, M Lacombe, D Hanauer, A Philip, N Schwartz, C Fontes, M

Citation: L. Villard et al., Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome, J MED GENET, 36(3), 1999, pp. 183-186

Authors: Villard, L Briault, S Lossi, AM Paringaux, C Belougne, J Colleaux, L Pincus, DR Woollatt, E Lespinasse, J Munnich, A Moraine, C Fontes, H Gecz, J

Citation: L. Villard et al., Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1, J MED GENET, 36(10), 1999, pp. 754-758

Authors: Lossi, AM Millan, JM Villard, L Orellana, C Cardoso, C Prieto, F Fontes, M Martinez, F

Citation: Am. Lossi et al., Mutation of the XNP/ATR-X gene in a family with severe mental retardation,spastic paraplegia and skewed pattern of X inactivation: Demonstration that the mutation is involved in the inactivation bias, AM J HU GEN, 65(2), 1999, pp. 558-562